Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGTCTCAGGAACCTACGACATACT[C/T]CCTTTTCCTATTCCTTTTTCTGAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607038 | ||||||||||||||||||||
Literature Links: |
OTOA PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
OTOA - otoancorin | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001161683.1 | 406 | Intron | NP_001155155.1 | |||
NM_144672.3 | 406 | Missense Mutation | TCC,TTC | S,F 9 | NP_653273.3 | |
NM_170664.2 | 406 | Intron | NP_733764.1 | |||
XM_011545747.2 | 406 | Missense Mutation | TCC,TTC | S,F 9 | XP_011544049.1 | |
XM_011545748.2 | 406 | Intron | XP_011544050.2 | |||
XM_017022950.1 | 406 | Missense Mutation | TCC,TTC | S,F 9 | XP_016878439.1 | |
XM_017022951.1 | 406 | Intron | XP_016878440.1 |